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Internal ID UUID644038b620e51090163095
Scientific name Alnus hirsuta
Authority (Spach) Rupr.
First published in Bull. Cl. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 15: 376 (1857)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among the Ainu of Hokkaido, the powdered inner bark is drunk as a mild decoction for gut troubles and fever (Hansson, 1998). In Korea, inner bark and young leaves are taken as teas or short decoctions for diarrhea, gut inflammation, and urogenital discomfort (Kim, 2003; Kim, 1982). Russian taiga peoples of southeastern Siberia also prepare a bark decoction as an internal remedy for diarrhea and sore throats (Sillanpää & Niemeyer, 2010). The species is distinguished in East Asian pharmacopoeial writing as a specific astringent (Kang & You, 1994; Korean Pharmacopoeia, 1997).

A practical, well‑tolerated preparation is a short bark decoction. Use 6–8 g of dried inner bark (broken or ground) with 250 ml of water, bring to a boil, then simmer 10–15 minutes, strain, and cool to a warm tea. Two or three cups a day are common in traditional practice for short‑term use during gut upset. Short‑term use of this bark decoction is reasonable, but reliable long‑term dosing data are lacking; as a simple guide, many herbalists limit a bark tea like this to a few consecutive days (Kang & You, 1994). Safety notes: not recommended for pregnancy or in people with known hypersensitivity to Betulaceae. Use caution in children.

The bark is rich in ellagitannins and condensed tannins (gallotannins such as casuarictin; proanthocyanidins), with flavonoids like quercetin and its glycosides, and triterpenoids including betulin and betulinic acid (Okuyama, 1993; Saijyo et al., 2008). These constituents are consistent with astringent and tissue‑tonic activities often described in the historical accounts.

A mild bark tea remains available in some East Asian markets, and a limited number of studies continue to screen Alnus hirsuta extracts for anti‑inflammatory and antimicrobial activity, though clinical trials in humans are still sparse (Lee et al., 2011; Lee et al., 2015).

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Alnus sibirica f. hirsutoides Koidz. Bot. Mag. (Tokyo) 27: 145 1913
Alnus tinctoria var. microphylla Nakai Bot. Mag. (Tokyo) 42: 17 (1928)
Alnus tinctoria var. velutina H.Hara Bot. Mag. (Tokyo) 48: 805. 1934
Alnus tinctoria f. hirsutoides (Koidz.) H.Hara Bot. Mag. (Tokyo) 48: 804 1934
Alnus tinctoria var. glabra Callier Repert. Spec. Nov. Regni Veg. 10: 233. 1911
Alnus sibirica var. tinctoria (Sarg.) Koidz. Bot. Mag. (Tokyo) 27: 145. 1913
Alnus sibirica f. obtusiloba Koidz. Bot. Mag. (Tokyo) 27: 145 1913
Alnus sibirica f. acutiloba Koidz. Bot. Mag. (Tokyo) 27: 145 1913
Alnus sibirica f. glabra (Callier) Koidz. Bot. Mag. (Tokyo) 27: 145 1913
Alnus tinctoria f. acutiloba (Koidz.) H.Hara Bot. Mag. (Tokyo) 48: 805 1934
Alnus hirsuta f. macrophylla Callier Repert. Spec. Nov. Regni Veg. 10: 233 1911
Alnus tinctoria var. obtusiloba Callier Repert. Spec. Nov. Regni Veg. 10: 233. 1911
Alnus tinctoria var. mandschurica Callier Repert. Spec. Nov. Regni Veg. 10: 233. 1911
Alnus hirsuta f. inokumae (Murai & Kusaka) H.Ohba Fl. Japan 2a: 29 (2006)
Alnus hirsuta f. sibirica (Spach) H.Ohba Fl. Japan 2a: 29 (2006)
Alnus hirsuta var. microphylla (Nakai) Tatew. Res. Bull. Coll. Exp. Forests Coll. Agric. Hokkaido Imp. Univ. 7: 189. 1932
Alnus hirsuta var. sibirica (Spach) C.K.Schneid. Pl. Wilson. 2: 498 1916
Alnus incana subsp. hirsuta (Spach) Á.Löve & D.Löve Bot. Not. 128: 505 (1975 publ. 1976)
Alnus incana var. hirsuta Spach Ann. Sci. Nat., Bot. II, 15: 207 1841
Alnus incana var. sibirica Spach Ann. Sci. Nat., Bot. , sér. 2, 15: 207 (1841)
Alnus incana var. tinctoria (Sarg.) H.J.P.Winkl. Pflanzenr. IV, 61: 123. 1904
Alnus inokumae Murai & Kusaka Bull. Gov. Forest Exp. Sta. 141: 158, 166 (1962)
Alnus sibirica (Spach) Turcz. ex Kom. Trudy Imp. S.-Peterburgsk. Bot. Sada 22: 57. 1903 (1903)
Alnus sibirica var. hirsuta (Spach) Koidz. Bot. Mag. (Tokyo) 27: 144 1913
Alnus sibirica var. oxyloba C.K.Schneid. Ill. Handb. Laubholzk. 2: 891. 1912
Alnus sibirica var. paucinervis C.K.Schneid. Ill. Handb. Laubholzk. 2: 891. 1912
Alnus tinctoria Sarg. Gard. & Forest 10: 472 (1897)
Alnus sibirica Fisch. ex Turcz. Bull. Soc. Imp. Naturalistes Moscou 11(1): 101. 1838 ; 27. (1854) I. 406
Alnus incana var. glauca (F.Michx.) Loudon Arbor. Frutic. Brit. 3: 1688. 1838
Alnus incana subsp. tchangbokii Chin S.Chang & H.Kim Forest Sci. Technol. (S. Korea) 7: 44 (2011)
Alnus incana f. hirsuta Regel Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 , 4(4): 136 (1861)
Alnus incana var. glauca Regel Nouv. Mém. Soc. Imp. Naturalistes Moscou 13(2): 154 (1861)
Alnus viridis var. sibirica (Spach) Regel Bull. Soc. Imp. Naturalistes Moscou 38(II): 422 (1865)

Common names Top

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Language Common/alternative name
English siberian alder
English manchurian alder
Azerbaijani yumşaqtüklü qızılağac
Icelandic hæruölur
Korean 물오리나무
Dutch olsza szorstka
Polish olsza szorstka
Russian Ольха шерстистая
Russian Ольха пушистая
Turkish mançurya kızılağacı
Chinese 旱冬瓜
Chinese 色赤杨
Chinese 辽东桤木

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000945674
Tropicos 3600204
KEW urn:lsid:ipni.org:names:77176842-1
The Plant List kew-6410
PaleoBotany 70089
Open Tree Of Life 639096
Observations.org 128041
NCBI Taxonomy 109061
IUCN Red List 194610
IPNI 294926-1
iNaturalist 437257
GBIF 2876105
EPPO ALUHI
EOL 1145867
Elurikkus 2675
USDA GRIN 2450
Plantarium 2290
PFAF Alnus hirsuta

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Worldwide forest surveys reveal forty-three new species in Phytophthora major Clade 2 with fundamental implications for the evolution and biogeography of the genus and global plant biosecurity Jung T, Milenković I, Balci Y, Janoušek J, Kudláček T, Nagy ZÁ, Baharuddin B, Bakonyi J, Broders KD, Cacciola SO, Chang TT, Chi NM, Corcobado T, Cravador A, Đorđević B, Durán A, Ferreira M, Fu CH, Garcia L, Hieno A, Ho HH, Hong C, Junaid M, Kageyama K, Kuswinanti T, Maia C, Májek T, Masuya H, Magnano di San Lio G, Mendieta-Araica B, Nasri N, Oliveira LS, Pane A, Pérez-Sierra A, Rosmana A, Sanfuentes von Stowasser E, Scanu B, Singh R, Stanivuković Z, Tarigan M, Thu PQ, Tomić Z, Tomšovský M, Uematsu S, Webber JF, Zeng HC, Zheng FC, Brasier CM, Horta Jung M Stud Mycol 27-Feb-2024
PMCID:PMC11003442
doi:10.3114/sim.2024.107.04
PMID:38600961
Classification, biosynthesis, and biological functions of triterpene esters in plants Liu J, Yin X, Kou C, Thimmappa R, Hua X, Xue Z Plant Commun 13-Feb-2024
PMCID:PMC11009366
doi:10.1016/j.xplc.2024.100845
PMID:38356259
Chemical Epigenetic Regulation Secondary Metabolites Derived from Aspergillus sydowii DL1045 with Inhibitory Activities for Protein Tyrosine Phosphatases Shi X, Li X, He X, Zhang D, Quan C, Xiu Z, Dong Y Molecules 31-Jan-2024
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Fine-Root Distribution and Soil Physicochemical Property Variations in Four Contrasting Urban Land-Use Types in South Korea Tran LT, An JY, Carayugan MB, Hernandez JO, Rahman SA, Youn WB, Carvalho JI, Jo MS, Han SH, Nguyen HH, Park BB Plants (Basel) 07-Jan-2024
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doi:10.3390/plants13020164
PMID:38256718
Evolution of masting in plants is linked to investment in low tissue mortality Journé V, Hacket-Pain A, Bogdziewicz M Nat Commun 02-Dec-2023
PMCID:PMC10693562
doi:10.1038/s41467-023-43616-1
PMID:38042862
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PMCID:PMC10668636
doi:10.3390/ani13223433
PMID:38003051
Distribution, Effect, and Control of Exotic Plants in Republic of Korea Lim BS, Seok JE, Lim CH, Kim GS, Shin HC, Lee CS Biology (Basel) 06-Jun-2023
PMCID:PMC10294914
doi:10.3390/biology12060826
PMID:37372111
Betula mcallisteri sp. nov. (sect. Acuminatae, Betulaceae), a new diploid species overlooked in the wild and in cultivation, and its relation to the widespread B. luminifera Zhang H, Ding J, Holstein N, Wang N Front Plant Sci 23-May-2023
PMCID:PMC10268003
doi:10.3389/fpls.2023.1113274
PMID:37324661
Diarylheptanoids/sorafenib as a potential anticancer combination against hepatocellular carcinoma: the p53/MMP9 axis of action Elmetwalli A, Diab T, Albalawi AN, El-Naggar SA, El‑Far AH, Ghedan AR, Alamri ES, Salama AF Naunyn Schmiedebergs Arch Pharmacol 05-May-2023
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PMID:37145126
Cluster Composition of Anemophilous Plant Pollen Entering the Atmosphere Golovko VV, Zueva GA, Kiseleva TI 15-Dec-2022
PMCID:PMC9753010
doi:10.1134/S1024856022060136
Environmental stress - what can we learn from chlorophyll a fluorescence analysis in woody plants? A review Swoczyna T, Kalaji HM, Bussotti F, Mojski J, Pollastrini M Front Plant Sci 14-Dec-2022
PMCID:PMC9795016
doi:10.3389/fpls.2022.1048582
PMID:36589121
Taxonomic Review of the Genus Caloptilia Hübner, 1825 (Lepidoptera: Gracillariidae) with Descriptions of Three New Species and Seven Newly Recorded Species from Korea Kim DS, Shin YM, Lee JY, Byun BK Insects 30-Nov-2022
PMCID:PMC9785696
doi:10.3390/insects13121107
PMID:36555017
Analysis of Components and Properties of Extractives from Alnus cremastogyne Pods from Different Provenances Chen G, Pan F, Gao Y, Li H, Qin X, Jiang Y, Qi J, Xie J, Jia S Molecules 12-Nov-2022
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PMCID:PMC9322912
doi:10.3390/plants11141880
PMID:35890514

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3aS,5aR,5bS,7aR,11aS,11bR,13aS,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 162943805 Click to see 424.70 unknown https://doi.org/10.1016/0031-9422(72)80041-4
> Phenylpropanoids and polyketides / Diarylheptanoids / Cyclic diarylheptanoids / Meta,para-diphenylether diarylheptanoids
(10R)-4,17-dimethoxy-2-oxatricyclo[13.2.2.13,7]icosa-1(17),3,5,7(20),15,18-hexaene-10,16-diol 10689752 Click to see 358.40 unknown https://doi.org/10.1248/BPB.30.810
4,17-Dimethoxy-2-oxatricyclo[13.2.2.13,7]icosa-1(17),3,5,7(20),15,18-hexaene-10,16-diol 44567146 Click to see 358.40 unknown https://doi.org/10.1248/BPB.30.810
Myricatomentogenin 10759713 Click to see 342.40 unknown https://doi.org/10.1248/BPB.30.810
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2S,4S,6R)-2-[(1S)-1-hydroxy-2-(4-hydroxyphenyl)ethyl]-6-(4-hydroxy-3-methoxyphenyl)oxan-4-ol 46184734 Click to see 360.40 unknown https://doi.org/10.1248/BPB.30.810
(3R)-1,7-Bis(3,4-Dihydroxyphenyl)-3-(Beta-D-Glucopyranosyl)Heptan-3-Ol 10097263 Click to see 494.50 unknown https://doi.org/10.1055/S-2000-8606
(4E)-1,7-Bis(3,4-dihydroxyphenyl)-4-hepten-3-one; 1,7-Bis-(3,4-dihydroxyphenyl)-4-hepten-3-one; Hirsutanone 66954880 Click to see C1=CC(=C(C=C1CCC=CC(=O)CCC2=CC(=C(C=C2)O)O)O)O 328.40 unknown https://doi.org/10.1248/BPB.30.810
1-(4-Hydroxyphenyl)-7-(4-hydroxy-3-methoxyphenyl)-4-hepten-3-one 78200757 Click to see 326.40 unknown https://doi.org/10.1248/BPB.30.810
1,7-Bis(3,4-dihydroxyphenyl)-5-(3,4,5-trihydroxyoxan-2-yl)oxyheptan-3-one 14707657 Click to see 478.50 unknown https://doi.org/10.1016/0031-9422(92)80049-K
https://doi.org/10.1055/S-2000-8606
2-[1-Hydroxy-2-(4-hydroxyphenyl)ethyl]-6-(4-hydroxy-3-methoxyphenyl)oxan-4-ol 44567145 Click to see 360.40 unknown https://doi.org/10.1248/BPB.30.810
2-[1,7-Bis(3,4-dihydroxyphenyl)heptan-3-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 75168353 Click to see C1=CC(=C(C=C1CCCCC(CCC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 494.50 unknown https://doi.org/10.1055/S-2000-8606
2-[1,7-Bis(3,4-dihydroxyphenyl)heptan-3-yloxy]oxane-3,4,5-triol 74202880 Click to see 464.50 unknown https://doi.org/10.1055/S-2000-8606
7-(4-Hydroxy-3-methoxy-phenyl)-1-(4-hydroxy-phenyl)-hept-4-en-3-one 637455 Click to see 326.40 unknown https://doi.org/10.1248/BPB.30.810
Hirsutal 13347317 Click to see C1=CC(=C(C=C1CCC(CC(=O)CCC2=CC(=C(C=C2)O)O)O)O)O 346.40 unknown https://doi.org/10.1248/BPB.30.810
https://doi.org/10.1055/S-2000-8606
Hirsutanonol 9928190 Click to see 346.40 unknown https://doi.org/10.1248/BPB.23.517
https://doi.org/10.1007/BF02977009
https://doi.org/10.1007/BF02976466
https://doi.org/10.1248/BPB.30.810
https://doi.org/10.1055/S-2000-8606
Hirsutenone 637394 Click to see 328.40 unknown https://doi.org/10.1248/BPB.30.810
Oregonin 14707658 Click to see 478.50 unknown https://doi.org/10.1007/BF02977009
https://doi.org/10.1055/S-2000-8606
https://doi.org/10.1248/BPB.23.517
https://doi.org/10.1016/0031-9422(92)80195-K
https://doi.org/10.1016/0031-9422(92)80049-K
https://doi.org/10.1007/BF02976608
https://doi.org/10.1007/BF02976466
Rubranoside B 24011643 Click to see 464.50 unknown https://doi.org/10.1055/S-2000-8606
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.3724/SP.J.1009.2012.00084
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
(2S,3S,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 44259219 Click to see 478.40 unknown https://doi.org/10.3724/SP.J.1009.2012.00084
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.3724/SP.J.1009.2012.00084
> Phenylpropanoids and polyketides / Tannins
[4,5-Dihydroxy-3,6-bis[(3,4,5-trihydroxybenzoyl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 14284610 Click to see 636.50 unknown https://doi.org/10.1016/0031-9422(92)80049-K
1,2,6-Tri-O-Galloyl-Beta-D-Glucose 440308 Click to see 636.50 unknown https://doi.org/10.1016/0031-9422(92)80049-K
1,2,6-Trigalloyl-beta-D-glucopyranose 3357644 Click to see 636.50 unknown https://doi.org/10.1016/0031-9422(92)80049-K
1,4,6-Tri-O-Galloyl-Beta-D-Glucose 10077822 Click to see 636.50 unknown https://doi.org/10.1016/0031-9422(92)80049-K
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11S,12R,13S,15R)-3,4,5,21,22,23-hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] 2-[[(1R,2S,19R,20R,22R)-7,8,9,12,13,14,20,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]-3,4,5-trihydroxybenzoate 16174839 Click to see 1721.20 unknown https://doi.org/10.1016/0031-9422(92)80049-K
[(10R,11S,12R,13S,15R)-3,4,5,21,22,23-hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] 3,4,5-trihydroxy-2-[[(1R,2S,19R,20S,22R)-7,8,9,12,13,14,29,30,33,34,35-undecahydroxy-4,17,25,38-tetraoxo-20-(3,4,5-trihydroxybenzoyl)oxy-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]benzoate 16174837 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C7C(C(O6)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O7)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C25)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1873.30 unknown https://doi.org/10.1016/0031-9422(92)80049-K
https://doi.org/10.1016/0031-9422(92)80195-K
[(2R,3S,4S,5R,6S)-6-(2,3-dihydroxy-5-methoxycarbonylphenoxy)-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 10097402 Click to see 498.40 unknown https://doi.org/10.1016/0031-9422(92)80049-K
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-12-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate 5153915 Click to see 786.60 unknown https://doi.org/10.1016/0031-9422(92)80049-K
[3,4,5,21,22,23-Hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] 3,4,5-trihydroxy-2-[[7,8,9,12,13,14,29,30,33,34,35-undecahydroxy-4,17,25,38-tetraoxo-20-(3,4,5-trihydroxybenzoyl)oxy-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]benzoate 16174836 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C7C(C(O6)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O7)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C25)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1873.30 unknown https://doi.org/10.1016/0031-9422(92)80049-K
[4-[(3S)-7-(3,4-dihydroxyphenyl)-5-oxo-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyheptyl]-2-hydroxyphenyl] 2-[[(1R,2S,19R,20S,22R)-7,8,9,12,13,14,20,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]-3,4,5-trihydroxybenzoate 162974824 Click to see C1C(C(C(C(O1)OC(CCC2=CC(=C(C=C2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C7C(C(O6)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C15)O)O)O)O)O)O)O)O)O)CC(=O)CCC1=CC(=C(C=C1)O)O)O)O)O 1413.10 unknown https://doi.org/10.1016/0031-9422(92)80049-K
[4-[(3S)-7-(3,4-dihydroxyphenyl)-5-oxo-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyheptyl]-2-hydroxyphenyl] 2-[[(1R,2S,19R,22R)-7,8,9,12,13,14,20,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]-3,4,5-trihydroxybenzoate 16183111 Click to see 1413.10 unknown https://doi.org/10.1016/0031-9422(92)80195-K
[4-[7-(3,4-Dihydroxyphenyl)-5-oxo-3-(3,4,5-trihydroxyoxan-2-yl)oxyheptyl]-2-hydroxyphenyl] 2-[(7,8,9,12,13,14,20,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl)oxy]-3,4,5-trihydroxybenzoate 162974822 Click to see 1413.10 unknown https://doi.org/10.1016/0031-9422(92)80049-K
[6-(2,3-Dihydroxy-5-methoxycarbonylphenoxy)-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 14428078 Click to see COC(=O)C1=CC(=C(C(=C1)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)O 498.40 unknown https://doi.org/10.1016/0031-9422(92)80049-K
2-[[(1R,2S,19R,20S,22R)-7,8,9,12,13,14,20,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]-3,4,5-trihydroxybenzoic acid 10033841 Click to see 952.60 unknown https://doi.org/10.1016/0031-9422(92)80049-K
alpha-Pedunculagin 13834142 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/0031-9422(92)80049-K
CID 14777390 14777390 Click to see 952.60 unknown https://doi.org/10.1016/0031-9422(92)80195-K
Degalloylrugosin F 16174838 Click to see 1721.20 unknown https://doi.org/10.1016/0031-9422(92)80195-K
https://doi.org/10.1016/0031-9422(92)80049-K
GlyTouCan:G69718UQ 9918701 Click to see 786.60 unknown https://doi.org/10.1016/0031-9422(92)80049-K
Pedunculagin 442688 Click to see 784.50 unknown https://doi.org/10.1016/0031-9422(92)80195-K
Pedunculagin I 492391 Click to see 784.50 unknown https://doi.org/10.1016/0031-9422(92)80049-K
Praecoxin A 14777391 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)O)O)O)O)O)O)O)O)O 952.60 unknown https://doi.org/10.1016/0031-9422(92)80049-K

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